Search results for "amines"

showing 10 items of 664 documents

Acetazolamide-M(II) [M(II) = Co(II), Ni(II), Cu(II)] complexes with ethylamine, diethylamine, triethylamine, and potassium hidroxide

1991

Abstract Complexes of Co(II), Ni(II), and Cu(II) with dideprotonated Acm are synthesized and characterized. Acm acts as bidentate ligand through the N-sulfonamido atom and the N-thiadiazole atom except for K6CoAcm4·6H2O in which Acm behaves as monodentate through the N-sulfonamido atom.

DenticityDiethylaminesPotassium CompoundsPotassiumInorganic chemistrychemistry.chemical_elementLigandsBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundNickelEthylaminesHydroxidesmedicineTriethylamineDiethylamineChemistrySpectrophotometry AtomicCobaltAcetazolamideSpectrophotometryPotassiumEthylamineAcetazolamideCoppermedicine.drugJournal of Inorganic Biochemistry
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Liquid Chromatographic Analysis of Amphetamine and Related Compounds in Urine Using Solid-Phase Extraction and 3,5-Dinitrobenzoyl Chloride for Deriva…

1997

A chromatographic method for the analysis of amphetamine and related compounds in urine using 3,5-dinitrobenzoyl chloride (3,5-DNB) as a labeling reagent is presented. This assay is based on the employment of solid-phase extraction (SPE) cartridges for sample cleanup and derivatization. Experimental conditions are optimized for the simultaneous derivatization of ephedrine, norephedrine, pseudoephedrine, beta-phenylethylamine, amphetamine, methamphetamine, and 3-phenylpropylamine. The derivatives formed are separated in a LiChrospher 1000 RP18 (125 x 4-mm i.d., 5-microns film thickness) analytical column using a water-acetonitrile gradient elution and detected at 254 nm. Derivatization in C1…

Detection limitAnalyteChromatographyAmphetaminesGeneral MedicinePseudoephedrineHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryNitrobenzoatesReagentmedicineIndicators and ReagentsSolid phase extractionEphedrineDerivatizationChromatography High Pressure Liquidmedicine.drugJournal of Chromatographic Science
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Urine polyamines determination using dansyl chloride derivatization in solid-phase extraction cartridges and HPLC

1999

The derivatization of biogenic amines such as putrescine, cadaverine, spermidine and spermine with dansyl chloride in solid phase extraction cartridges is described. Different types of filling materials were tested in order to have the highest retention of the different analytes. The best results were obtained by using C18 cartridges. The optimal conditions were: amine solution buffered at pH 12, 2 mM dansyl chloride (acetone-bicarbonate solution 20 mM (pH 9-9.5), 2 + 3 v/v) as reagent concentration, room temperature and 30 min reaction time. The developed procedure was applied to the determination of these polyamines in urine samples from healthy controls and cancer patients using HPLC wit…

Detection limitCadaverineChromatographyBiogenic PolyaminesDansyl chlorideBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryNeoplasmsReagentBiomarkers TumorElectrochemistryPutrescineHumansEnvironmental ChemistrySolid phase extractionDerivatizationChromatography High Pressure LiquidSpectroscopyThe Analyst
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A microanalytical method for ammonium and short-chain primary aliphatic amines using precolumn derivatization and capillary liquid chromatography.

2007

Abstract A new microscale method is presented for the determination of ammonium and primary short-chain aliphatic amines (methylamine, ethylamine, propylamine, n -butylamine and n -pentylamine) in water. The assay uses precolumn derivatization with the reagent o -phthaldialdehyde (OPA) in combination with the thiol N -acetyl- l -cysteine (NAC), and capillary liquid chromatography with UV detection at 330 nm. The described method is very simple and rapid as no preconcentration of the analytes is necessary, and the volume of sample required is only 0.1 mL. Under the proposed conditions good linearity has been obtained up to a concentration of the analytes of 10.0 mg L −1 , the limits of detec…

Detection limitChromatographyChemistryButylamineOrganic ChemistryReproducibility of ResultsWaterPropylamineGeneral MedicineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryQuaternary Ammonium Compoundschemistry.chemical_compoundReagentEthylaminePentylamineAminesDerivatizationChromatography LiquidJournal of chromatography. A
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Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry Analysis of Carbosulfan, Carbofuran, 3-Hydroxycarbofuran, and Other Metabolites in …

2007

The potential of liquid chromatography quadrupole time-of-flight mass spectrometry (LC-QqTOF-MS) to identify and confirm carbosulfan and seven of its main metabolites (carbofuran, 3-hydroxycarbofuran, 3-ketocarbofuran, 3-hydroxy-7-phenol carbofuran, 3-keto-7-phenolcarbofuran, 7-phenolcarbofuran, dibutylamine) at trace levels from food is explored for the first time. The analytical method developed consists of pressurized liquid extraction (PLE) and LC-QqTOF-MS in positive ion mode, which attains unequivocal identification and quantification of the studied compounds in food, at levels well below of those of concern (0.05 mg/kg for the sum of carbosulfan, carbofuran, and 3-hydroxycarbofuran).…

Detection limitChromatographyMolecular StructureMetaboliteRepeatabilityButylaminesMass spectrometrySensitivity and SpecificityAnalytical ChemistryDibutylamineCarbofuranchemistry.chemical_compoundchemistrySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationCarbosulfanCarbamatesQuantitative analysis (chemistry)CarbofuranFood AnalysisChromatography LiquidAnalytical Chemistry
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In-tube solid-phase microextraction and liquid chromatography using a monolithic column for the selective determination of residual ethylenediamine i…

2009

The selective determination of the diamine ethylenediamine (EDA) in the presence of a higher amount of residual dimethylamine in cationic polymers has been developed. The strategy uses both a solution derivatization with a selective agent of primary amines such as o-phthaldialdehyde-N-acetyl-L-cysteine (OPA-NAC) and an in-tube solid-phase microextraction (IT-SPME) coupled to liquid chromatography (LC). A 70 cm long, 0.32 mm internal diameter, and 3 microm thick commercially available capillary column coated with 95% polydimethylsiloxane and 5% polydiphenylsiloxane was employed to replace the injection loop of a Rheodyne injection valve. A volume of 1 mL of derivatized sample was passed thro…

Detection limitChromatographyMonolithic HPLC columnPolydimethylsiloxaneCapillary actionPolymersCationic polymerizationSolid-phase microextractionEthylenediaminesAnalytical Chemistrychemistry.chemical_compoundchemistryChemical IndustryIndicators and ReagentsDerivatizationDimethylamineSolid Phase MicroextractionChromatography LiquidAnalytical chemistry
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Automated on-line in-tube solid-phase microextraction-assisted derivatization coupled to liquid chromatography for quantifying residual dimethylamine…

2008

Abstract A method for the analysis of dimethylamine (DMA) by automated in-tube solid-phase microextraction (IT-SPME)-supported chemical derivatization coupled with high-performance liquid chromatography was developed. Extraction, derivatization and desorption were studied by using a capillary coated with 95% polydimethylsiloxane and 5% polydiphenylsiloxane. Solution derivatization and automated IT-SPME derivatization using 9-fluorenylmethyl chloroformate (FMOC) were compared. The proposed procedure provided adequate linearity, accuracy and precision in the 0.2–2.0 μg/mL concentration interval, and the limit of detection (LOD) was 50 ng/mL. The main advantages of the proposed procedure are: …

Detection limitChromatographyPolymersChemistryOrganic ChemistryGeneral MedicineChloroformateSolid-phase microextractionOnline SystemsBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundReagentSample preparationDerivatizationDimethylamineDimethylaminesSolid Phase MicroextractionChromatography Liquid
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Derivatization of tertiary amphetamines with 9-fluorenylmethyl chloroformate for liquid chromatography: determination of N-methylephedrine.

2000

The fluorogenic reagent 9-fluorenylmethyl chloroformate (FMOC) was evaluated for the derivatization of tertiary amphetamines prior to liquid chromatographic analysis. Conditions for the derivatization were investigated, including the reaction time, the derivatization reagent concentration and the pH, using N-methylephedrine as a model compound. On the basis of these studies, a method for the quantification of N-methylephedrine is presented. The method involves derivatization with FMOC at ambient temperature and separation of the derivatives formed on a LiChrospher C18, 5 μm, 125 × 4 mm id column using acetonitrile–water gradient elution. The proposed procedure shows good linearity, accuracy…

Detection limitEphedrineReproducibilityFluorenesChromatographyAmphetaminesChloroformateBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryEvaluation Studies as TopicReagentElectrochemistryEnvironmental ChemistryGradient elutionIndicators and ReagentsDerivatizationN-MethylephedrineSpectroscopyChromatography LiquidThe Analyst
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Liquid chromatographic determination of trimethylamine in water.

2004

A method for the selective determination of trimethylamine (TMA) in aqueous matrices by liquid chromatography is reported. The proposed procedure is based on the derivatization of the analyte with 9-fluorenylmethyl chloroformate (FMOC) in a precolumn (Hypersil C18, 30 microm, 20 mm x 2.1 mm i.d.) connected on-line to the analytical column (LiChrosphere 100 RP18, 5 microm, 125 mm x 4 mm i.d.). Gradient elution was performed with a mixture of acetonitrile-water-0.05 M borate buffer (pH 9.0). The method has been applied to the direct determination of TMA in water within the 0.25-10.0 microg/ml concentration interval, and can also be adapted to the determination of TMA over the range 0.05-1.0 m…

Detection limitFluorenesChromatographyTertiary amineChemistryOrganic ChemistryWaterTrimethylamineGeneral MedicineReversed-phase chromatographyChloroformateSensitivity and SpecificityBiochemistryAnalytical ChemistryMethylamineschemistry.chemical_compoundSample preparationSolid phase extractionDerivatization
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Quantitation of talinolol in rat plasma by LC-MS-MS.

2010

The aim of this study was to develop and validate an assay based on liquid chromatography-tandem mass spectrometry to quantitate talinolol in rat plasma. After a simple protein precipitation step, separation was performed by reversed-phase liquid chromatography using gradient elution with acetonitrile-water-formic acid. Electrospray ionization in the positive ion mode with multiple reaction monitoring was used to analyze talinolol employing propranolol as internal standard. The calibration curve for talinolol was linear over the concentration range 1-250 ng/mL with a correlation coefficient0.995. The method was sensitive (limit of quantitation, 1 ng/mL) and had acceptable accuracy (85-115% …

Detection limitMaleSpectrometry Mass Electrospray IonizationChromatographyElectrospray ionizationSelected reaction monitoringAnalytical chemistryGeneral MedicineReversed-phase chromatographyMass spectrometryHigh-performance liquid chromatographyAnalytical ChemistryRatsPropanolamineschemistry.chemical_compoundchemistryProtein precipitationAnimalsRats WistarAntihypertensive AgentsChromatography High Pressure LiquidTalinololChromatography LiquidJournal of chromatographic science
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